510(k) K032661 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
ACON QUICK-CHECK II HOME PREGNANCY TEST DEVICE (CASSETTE)
| Applicant | ACON Laboratories, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Oct 14, 2003 |
| Received | Aug 28, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032661
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.